The HLA-C*04:01/KIR2DS4 gene combination and human leukocyte antigen alleles with high population frequency drive rate of HIV disease progression


Por: Olvera, A, Perez-Alvarez, S, Lbarrondo, J, Ganoza, C, Lama, JR, Lucchetti, A, Cate, S, Hildebrand, W, Bernard, N, Gomez, L, Sanchez, J and Brander, C

Publicada: 13 mar 2015
Resumen:
Objective: The objective of this study is to identify human leukocyte antigen (HLA) class I and killer-cell immunoglobulin-like receptor (KIR) genotypes associated with different risks for HIV acquisition and HIV disease progression. Design: A cross-sectional study of a cohort of 468 high-risk individuals (246 HIV-positive and 222 HIV-negative) from outpatient clinics in Lima (Peru). Methods: The cohort was high-resolution HLA and KIR-typed and analysed for potential differences in single-allele frequencies and allele combinations between HIV-positive and HIV-negative individuals and for associations with HIV viral load and CD4(+) cell counts in infected individuals. Results: HLA class I alleles associated with a lack of viral control had a significantly higher population frequency than relatively protective alleles (P = 0.0093), in line with a rare allele advantage. HLA-A*02 : 01 and HLA-C*04 : 01 were both associated with high viral loads (P = 0.0313 and 0.0001, respectively) and low CD4(+) cell counts (P = 0.0008 and 0.0087, respectively). Importantly, the association between HLA-C*04 : 01 and poor viral control was not due to its linkage disequilibrium with other HLA alleles. Rather, the coexpression of its putative KIR ligand KIR2DS4f was critically linked to elevated viral loads. Conclusion: These results highlight the impact of population allele frequency on viral control and identify a novel association between HLA-C*04 : 01 in combination with KIR2DS4f and uncontrolled HIV infection. Our data further support the importance of the interplay of markers of the adaptive and innate immune system in viral control. Copyright (C) 2015 Wolters Kluwer Health, Inc. All rights reserved.

Filiaciones:
:
 Hosp Germans Trias, IrsiCaixa AIDS Res Inst HIVACAT, Barcelona, Spain

Perez-Alvarez, S:
 Hosp Germans Trias, IrsiCaixa AIDS Res Inst HIVACAT, Barcelona, Spain

 Univ Autonoma Barcelona, E-08193 Barcelona, Spain

Lbarrondo, J:
 Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA

Ganoza, C:
 Asociac Civil IMPACTA Salud & Educ, Lima, Peru

Lama, JR:
 Asociac Civil IMPACTA Salud & Educ, Lima, Peru

 Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA

Lucchetti, A:
 Asociac Civil IMPACTA Salud & Educ, Lima, Peru

Cate, S:
 Univ Oklahoma, Hlth Sci Ctr, Oklahoma City, OK USA

Hildebrand, W:
 Univ Oklahoma, Hlth Sci Ctr, Oklahoma City, OK USA

Bernard, N:
 McGill Univ, Ctr Hlth, Res Inst, Montreal, PQ, Canada

Gomez, L:
 Univ Politecn Cataluna, Dept Estadist & Invest Operat, Barcelona, Spain

Sanchez, J:
 Asociac Civil IMPACTA Salud & Educ, Lima, Peru

 Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA

:
 Hosp Germans Trias, IrsiCaixa AIDS Res Inst HIVACAT, Barcelona, Spain

 Univ Autonoma Barcelona, E-08193 Barcelona, Spain

 ICREA, Barcelona, Spain

 Univ Vic UVIC UCC, Vic, Spain
ISSN: 02699370





AIDS
Editorial
Lippincott Williams & Wilkins Ltd., TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 29 Número: 5
Páginas: 507-517
WOS Id: 000350766400001
ID de PubMed: 25715101
imagen Green Submitted

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